Otisur
Otisur
Authorised
- Miconazole nitrate
- Prednisolone acetate
- POLYMYXIN B SULFATE
Product identification
Medicine name:
Otisur
Otisur vet 23,0 mg/ml + 5,0 mg/ml + 5500 IU/ml korvatipat, suspensio
Active substance:
- Miconazole nitrate
- Prednisolone acetate
- POLYMYXIN B SULFATE
Target species:
-
Dog
-
Cat
Route of administration:
-
Auricular use
-
Cutaneous use
Product details
Active substance and strength:
-
Miconazole nitrate23.00milligram(s)1.00millilitre(s)
-
Prednisolone acetate5.00milligram(s)1.00millilitre(s)
-
POLYMYXIN B SULFATE5500.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Ear drops, suspension
Withdrawal period by route of administration:
-
Auricular use
-
Dog
-
Cat
-
-
Cutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QS02CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Finland
Package description:
- 30 ml white low-density polyethylene squeeze dropper bottle with a white, high-density polyethylene cap (screw fit), and a white, low-density polyethylene dropper.
- 15 ml white low-density polyethylene squeeze dropper bottle with a white, high-density polyethylene cap (screw fit), and a white, low-density polyethylene dropper.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Finnish Medicines Agency
Authorisation number:
- 39033
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0659/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovenia
-
Spain
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
Finnish (PDF)
Published on: 29/05/2023
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Finnish (PDF)
Published on: 29/05/2023
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